2-(1-Methyl-6-phenacylpiperidin-3-yl)-1-phenylethanone

Details

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Internal ID 1aef130e-13dc-4e7e-8927-3dd44d32cedf
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 2-(1-methyl-6-phenacylpiperidin-3-yl)-1-phenylethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H25NO2/c1-23-16-17(14-21(24)18-8-4-2-5-9-18)12-13-20(23)15-22(25)19-10-6-3-7-11-19/h2-11,17,20H,12-16H2,1H3
InChI Key AHSYGTGCCMEKRI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H25NO2
Molecular Weight 335.40 g/mol
Exact Mass 335.188529040 g/mol
Topological Polar Surface Area (TPSA) 37.40 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1-Methyl-6-phenacylpiperidin-3-yl)-1-phenylethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9703 97.03%
Caco-2 + 0.8575 85.75%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7752 77.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior + 0.8337 83.37%
P-glycoprotein inhibitior - 0.4845 48.45%
P-glycoprotein substrate - 0.6987 69.87%
CYP3A4 substrate - 0.5868 58.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6273 62.73%
CYP3A4 inhibition - 0.8498 84.98%
CYP2C9 inhibition - 0.8115 81.15%
CYP2C19 inhibition - 0.5986 59.86%
CYP2D6 inhibition - 0.6549 65.49%
CYP1A2 inhibition + 0.5443 54.43%
CYP2C8 inhibition - 0.9184 91.84%
CYP inhibitory promiscuity - 0.9202 92.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6504 65.04%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9823 98.23%
Skin irritation - 0.6615 66.15%
Skin corrosion - 0.8308 83.08%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9240 92.40%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.5737 57.37%
skin sensitisation - 0.9026 90.26%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6116 61.16%
Acute Oral Toxicity (c) III 0.7148 71.48%
Estrogen receptor binding + 0.6845 68.45%
Androgen receptor binding - 0.5918 59.18%
Thyroid receptor binding - 0.7371 73.71%
Glucocorticoid receptor binding - 0.7196 71.96%
Aromatase binding - 0.5984 59.84%
PPAR gamma - 0.8431 84.31%
Honey bee toxicity - 0.9753 97.53%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.6928 69.28%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.60% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.54% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.42% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.07% 98.95%
CHEMBL4072 P07858 Cathepsin B 86.62% 93.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.95% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.37% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.35% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Lobelia chinensis
Lobelia inflata

Cross-Links

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PubChem 5319058
NPASS NPC200837